ClinVar Miner

Submissions for variant NM_000256.3(MYBPC3):c.1335G>C (p.Thr445=)

dbSNP: rs727503205
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV000781625 SCV000919810 likely benign not specified 2019-08-29 criteria provided, single submitter clinical testing
Invitae RCV002535697 SCV003229697 likely benign Hypertrophic cardiomyopathy 2021-12-02 criteria provided, single submitter clinical testing

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